ENST00000269980.7:c.257G>T
MANE Select
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ENSP00000269980.2:p.Gly86Val
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ENST00000269980.6:c.257G>T
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ENSP00000269980.2:p.Gly86Val
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ENST00000457836.6:c.191G>T
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ENSP00000416000.2:p.Gly64Val
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ENST00000538423.5:n.277G>T
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ENST00000540732.3:c.359G>T
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ENSP00000443246.1:p.Gly120Val
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ENST00000541315.1:c.64G>T
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ENST00000542943.5:c.257G>T
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ENSP00000440345.1:p.Gly86Val
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ENST00000595085.5:c.257G>T
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ENSP00000471150.2:p.Gly86Val
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ENST00000604424.1:n.499G>T
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NM_000709.3:c.257G>T
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NP_000700.1:p.Gly86Val
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NM_001164783.1:c.257G>T
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NP_001158255.1:p.Gly86Val
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NM_000709.4:c.257G>T
MANE Select
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NP_000700.1:p.Gly86Val
|
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NM_001164783.2:c.257G>T
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NP_001158255.1:p.Gly86Val
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